Enhanced fertility programme: developing an accessible, safe and cost-effective digital solution to improve fertility
Not Applicable
- Conditions
- Primary and Secondary Infertility, ovulatory disorders, male factor and unexplained infertilityUrological and Genital Diseases
- Registration Number
- ISRCTN12487925
- Lead Sponsor
- inFertile Life
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Ongoing
- Sex
- All
- Target Recruitment
- 128
Inclusion Criteria
1. Heterosexual couples or women seeking fertility treatment at one of the trial participating centres
2. Age 20-37
3. English speaking
4. Capacity to understand and use a computer with internet access
5. Diagnosed with primary or secondary infertility related to unexplained infertility, ovulatory disorders or male factor infertility
Exclusion Criteria
1. Any anatomical congenital gynaecological or urological abnormalities
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <br> Measured at: baseline, 6 weeks, 12 weeks, 18 weeks and 24 weeks through online questionnaire completed by participants:<br> 1. Pregnancy status: nominal scale (yes/no)<br> 2. Adherence to healthy lifestyles: Likert scale (Very good, good, nor good nor bad, poor, very poor)<br> 3. Ability to cope with treatment: Likert scale (completely, a great deal, moderately, not much, nor at all).<br> 4. Patient satisfaction: likert scale (extremely likely, likely, neither, unlikely, extremely unlikely).<br> 5. Quality of life: FertiQoL<br>
- Secondary Outcome Measures
Name Time Method <br> Measured at 6 months through online questionnaire completed by participants:<br> 1. Accessibility to health promotion strategies: Likert scale (completely, a great deal, moderately, not much, not at all).<br> 2. Inequality in fertility care: Likert scale (completely, a great deal, moderately, not much, not at all).<br>